Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox4 |
T |
C |
1: 58,301,730 (GRCm39) |
C1101R |
probably damaging |
Het |
Atp8b5 |
T |
C |
4: 43,357,016 (GRCm39) |
I588T |
probably damaging |
Het |
Bahd1 |
C |
T |
2: 118,746,887 (GRCm39) |
P169S |
probably damaging |
Het |
Cd164l2 |
T |
A |
4: 132,950,986 (GRCm39) |
V147E |
probably damaging |
Het |
Celsr3 |
G |
A |
9: 108,723,262 (GRCm39) |
|
probably null |
Het |
Cr2 |
T |
C |
1: 194,836,482 (GRCm39) |
T894A |
probably damaging |
Het |
Crtc3 |
T |
C |
7: 80,239,696 (GRCm39) |
D552G |
probably damaging |
Het |
Cspg4b |
A |
T |
13: 113,455,733 (GRCm39) |
N593I |
probably damaging |
Het |
Cyp2c50 |
A |
G |
19: 40,079,083 (GRCm39) |
E142G |
probably damaging |
Het |
Dcstamp |
A |
G |
15: 39,617,620 (GRCm39) |
I10V |
probably benign |
Het |
Gm44501 |
T |
A |
17: 40,887,507 (GRCm39) |
F8L |
unknown |
Het |
Gpr179 |
T |
C |
11: 97,226,537 (GRCm39) |
S1873G |
probably benign |
Het |
Gprin2 |
C |
A |
14: 33,916,754 (GRCm39) |
A339S |
probably benign |
Het |
Gucy1b2 |
T |
A |
14: 62,649,038 (GRCm39) |
I513F |
possibly damaging |
Het |
Ighv5-6 |
T |
A |
12: 113,589,208 (GRCm39) |
R91* |
probably null |
Het |
Igtp |
G |
A |
11: 58,097,824 (GRCm39) |
V332I |
possibly damaging |
Het |
Itfg1 |
G |
A |
8: 86,452,878 (GRCm39) |
P497S |
probably damaging |
Het |
Junb |
T |
C |
8: 85,704,517 (GRCm39) |
N181S |
possibly damaging |
Het |
Lama3 |
T |
C |
18: 12,614,145 (GRCm39) |
Y1305H |
probably benign |
Het |
Lrrcc1 |
A |
T |
3: 14,616,503 (GRCm39) |
N44I |
probably damaging |
Het |
Med15 |
A |
T |
16: 17,489,428 (GRCm39) |
|
probably benign |
Het |
Mkks |
T |
C |
2: 136,722,494 (GRCm39) |
E221G |
probably benign |
Het |
Mtmr10 |
T |
C |
7: 63,970,379 (GRCm39) |
V374A |
possibly damaging |
Het |
Muc5b |
G |
T |
7: 141,422,187 (GRCm39) |
C4441F |
possibly damaging |
Het |
Nlrp6 |
A |
G |
7: 140,501,694 (GRCm39) |
D87G |
probably damaging |
Het |
Ntng1 |
C |
A |
3: 110,051,124 (GRCm39) |
|
probably benign |
Het |
Padi1 |
G |
T |
4: 140,544,581 (GRCm39) |
|
probably benign |
Het |
Rxrg |
T |
C |
1: 167,452,596 (GRCm39) |
S133P |
probably benign |
Het |
Snx19 |
T |
C |
9: 30,339,192 (GRCm39) |
I110T |
probably benign |
Het |
Strap |
T |
C |
6: 137,726,334 (GRCm39) |
|
probably benign |
Het |
Tasor2 |
T |
C |
13: 3,631,831 (GRCm39) |
D890G |
probably benign |
Het |
Tgtp2 |
A |
T |
11: 48,950,179 (GRCm39) |
M131K |
probably damaging |
Het |
Tppp2 |
T |
C |
14: 52,156,868 (GRCm39) |
F82L |
probably damaging |
Het |
Ttc39c |
A |
G |
18: 12,863,126 (GRCm39) |
K397E |
possibly damaging |
Het |
Txlnb |
T |
TTA |
10: 17,714,745 (GRCm39) |
|
probably null |
Het |
Usp36 |
T |
A |
11: 118,176,621 (GRCm39) |
R66W |
probably damaging |
Het |
Vmn1r30 |
A |
T |
6: 58,412,118 (GRCm39) |
V238E |
probably damaging |
Het |
Vmn1r6 |
A |
G |
6: 56,980,174 (GRCm39) |
I279V |
probably benign |
Het |
Vmn2r61 |
G |
A |
7: 41,950,120 (GRCm39) |
D847N |
probably benign |
Het |
Zfp622 |
G |
A |
15: 25,987,137 (GRCm39) |
|
probably null |
Het |
Zfp963 |
T |
C |
8: 70,197,135 (GRCm39) |
I36V |
probably benign |
Het |
Zfy2 |
A |
G |
Y: 2,107,351 (GRCm39) |
Y428H |
possibly damaging |
Het |
|
Other mutations in Nim1k |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R1334:Nim1k
|
UTSW |
13 |
120,174,024 (GRCm39) |
missense |
probably benign |
0.05 |
R1782:Nim1k
|
UTSW |
13 |
120,173,687 (GRCm39) |
missense |
probably benign |
0.00 |
R2216:Nim1k
|
UTSW |
13 |
120,175,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R3710:Nim1k
|
UTSW |
13 |
120,173,635 (GRCm39) |
missense |
probably benign |
|
R4385:Nim1k
|
UTSW |
13 |
120,174,162 (GRCm39) |
missense |
probably damaging |
0.98 |
R4430:Nim1k
|
UTSW |
13 |
120,174,078 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4812:Nim1k
|
UTSW |
13 |
120,173,920 (GRCm39) |
missense |
probably benign |
|
R5383:Nim1k
|
UTSW |
13 |
120,189,335 (GRCm39) |
missense |
probably benign |
0.25 |
R5436:Nim1k
|
UTSW |
13 |
120,189,065 (GRCm39) |
intron |
probably benign |
|
R5511:Nim1k
|
UTSW |
13 |
120,189,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6682:Nim1k
|
UTSW |
13 |
120,173,724 (GRCm39) |
missense |
probably benign |
0.09 |
R6922:Nim1k
|
UTSW |
13 |
120,189,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R7053:Nim1k
|
UTSW |
13 |
120,189,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Nim1k
|
UTSW |
13 |
120,173,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R8168:Nim1k
|
UTSW |
13 |
120,174,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8333:Nim1k
|
UTSW |
13 |
120,174,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R8401:Nim1k
|
UTSW |
13 |
120,174,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Nim1k
|
UTSW |
13 |
120,175,807 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8515:Nim1k
|
UTSW |
13 |
120,173,986 (GRCm39) |
nonsense |
probably null |
|
R8540:Nim1k
|
UTSW |
13 |
120,175,718 (GRCm39) |
missense |
probably benign |
0.34 |
R8915:Nim1k
|
UTSW |
13 |
120,173,874 (GRCm39) |
missense |
probably benign |
0.10 |
R9227:Nim1k
|
UTSW |
13 |
120,174,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Nim1k
|
UTSW |
13 |
120,189,362 (GRCm39) |
missense |
probably benign |
|
Z1177:Nim1k
|
UTSW |
13 |
120,189,238 (GRCm39) |
missense |
probably benign |
0.02 |
|